HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235585Generated: October 30, 2026
Ethyl 2-(5-fluoro-2-nitrophenoxy)acetate → 7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-one
https://huagongshe.com/reaction/235585
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-(5-fluoro-2-nitrophenoxy)acetate | HCID 13752803 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-one | HCID 13731295 | 62.6% |
Reaction Steps
Iron powder (36.42 g) was suspended in 5% aqueous acetic acid (69 ml) and heated to 80° C. To the suspension, a solution of ethyl 5-fluoro-2-nitrophenoxyacetate (15.86 g) in acetic acid (65 ml) and ethyl acetate (65 ml) was dropwise added, and the resultant mixture was heated at 60° to 80° C. under reflux for 3 hours. After removal of residue by filtration, the filtrate was extracted with ethyl acetate. The extract was washed with water and sodium bicarbonate solution, dried and concentrated to give 7-fluoro-2H-1,4-benzoxazin-3(4H)-one (6.82 g). m.p., 186.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04640707 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-eff36f6230224334b85478f2010ece7d |
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| Source note | uspto-grants-1987_02 |
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